A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242888



Internal ID20809928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38818556..38819636hg38UCSC Ensembl
chr17:36974809..36975889hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593354
Supporting Variants
Samples
Known GenesCWC25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242888
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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